The effect of aluminum and water on the development of deformation fabrics of orthopyroxene

The effect of alumina and water solubility on the development of fabric in orthopyroxene in response to simple shear deformation has been investigated at a pressure of 1.5 GPa and a temperature of 1,100 °C using the D-DIA apparatus. The microstructure observations at these conditions indicate that dislocation glide is the dominant deformation mechanism. In MgSiO₃ enstatite and hydrous aluminous enstatite, partial dislocations bounding the stacking faults in [001] glide parallel to the (100) (or) the (100) [001] slip system. Electron backscattered diffraction analysis of anhydrous aluminous enstatite, however, indicates operation of the (010) [001] slip system, and microstructure analysis indicates dislocation movement involving [001] on both (100) and {210} planes. The strong covalent bonding induced by the occupation of M1 and T2 sites by Al could have restricted the glide on (100), activating slip on {210}. The resulting seismic anisotropies (~2 %) in orthopyroxene are weaker compared to olivine (~9.5 %), and reduced anisotropy can be expected if orthopyroxene coexists with olivine. Weak anisotropy observed in stable cratonic regions can be explained by the relatively high abundance of orthopyroxene in these rocks.     

How hydrological factors initiate instability in a model sandy slope

Knowledge of the mechanisms of rain‐induced shallow landslides can improve the prediction of their occurrence and mitigate subsequent sediment disasters. Here, we examine an artificial slope's subsurface hydrology and propose a new slope stability analysis that includes seepage force and the down‐slope transfer of excess shear forces. We measured pore water pressure and volumetric water content immediately prior to a shallow landslide on an artificial sandy slope of 32°: The direction of the subsurface flow shifted from downward to parallel to the slope in the deepest part of the landslide mass, and this shift coincided with the start of soil displacement. A slope stability analysis that was restricted to individual segments of the landslide mass could not explain the initiation of the landslide; however, inclusion of the transfer of excess shear forces from up‐slope to down‐slope segments improved drastically the predictability. The improved stability analysis revealed that an unstable zone expanded down‐slope with an increase in soil water content, showing that the down‐slope soil initially supported the unstable up‐slope soil; destabilization of this down‐slope soil was the eventual trigger of total slope collapse. Initially, the effect of apparent soil cohesion was the most important factor promoting slope stability, but seepage force became the most important factor promoting slope instability closer to the landslide occurrence. These findings indicate that seepage forces, controlled by changes in direction and magnitude of saturated and unsaturated subsurface flows, may be the main cause of shallow landslides in sandy slopes. Copyright © 2013 John Wiley & Sons, Ltd.     

Transport of oceanic nitrate from the continental shelf to the coastal basin in relation to the path of the Kuroshio

Hydrographic and biogeochemical observations were conducted along the longitudinal section from Ise Bay to the continental margin (southern coast of Japan) to investigate changes according to the Kuroshio path variations during the summer. The strength of the uplift of the cold deep water was influenced by the surface intrusion of the Kuroshio water to the shelf region. When the intrusion of the Kuroshio surface water to the shelf region was weak in 2006, the cold and NO₃⁻-rich shelf water intruded into the bottom layer in the bay from the shelf. This bottom intrusion was intensified by the large river discharge. The nitrogen isotope ratio (δ¹⁵N) of NO₃⁻ (4–5‰) in the bottom bay water was same as that in the deeper NO₃⁻ over the shelf, indicating the supply of new nitrogen to the bay. The warm and NO₃⁻-poor shelf water intruded into the middle layer via the mixing region at the bay mouth when the Kuroshio water distributed in the coastal areas off Ise Bay in 2005. The regenerated NO₃⁻ with isotopically light nitrogen (δ¹⁵N=−1‰) was supplied from the shelf to the bay. This NO₃⁻ is regenerated by the nitrification in the upper layer over the shelf. The contribution rate of regenerated NO₃⁻ over the shelf to the total NO₃⁻ in the subsurface chlorophyll maximum layer in the bay was estimated at 56% by a two-source mixing model coupled with the Rayleigh equation.     

Nitrogen isotopic discrimination by water column nitrification in a shallow coastal environment

Temporal changes in nitrogen isotopic composition (δ¹⁵N) of the NO₃ ⁻ pool in the water column below the pycnocline in Ise Bay, Japan were investigated to evaluate the effect of nitrification on the change in the δ¹⁵N in the water column. The δ¹⁵N of NO₃ ⁻ in the lower layers varied from −8.5‰ in May to +8.4‰ in July in response to the development of seasonal hypoxia and conversion from NH₄ ⁺ to NO₃ ⁻. The significantly ¹⁵N-depleted NO₃ ⁻ in May most likely arose from nitrification in the water column. The calculated apparent isotopic discrimination for water column nitrification (ɛ_nit = δ¹⁵N_substrate − δ¹⁵N_product) was 24.5‰, which lies within the range of previous laboratory-based estimates. Though prominent deficits of NO₃ ⁻ from hypoxic bottom waters due to denitrification were revealed in July, the isotopic discrimination of denitrification in the sediments was low (ɛ_denit = ∼1‰). δ¹⁵N_NO3 in the hypoxic lower layer mainly reflects the isotopic effect of water column nitrification, given that water column nitrification is not directly linked with sedimentary denitrification and the effect of sedimentary denitrification on the change in δ¹⁵N_NO3 is relatively small.     

Fluid inclusion evidence for rapid formation of the vapor-dominated zone at Sulphur Springs, Valles caldera, New Mexico, USA

Microthermometric measurements were obtained for 618 fluid inclusions in hydrothermal quartz, fluorite and calcite and magmatic quartz phenocrysts in intracaldera tuffs from the VC-2A core hole in order to study evolutionary processes of the Sulphur Springs hydrothermal system in the Valles caldera. Relatively high T_h values in samples from shallow depths indicate erosion of about 200 m of caldera fill since deposition of hydrothermal minerals at shallow depths in the Sulphur Springs hydrothermal system, accompanied by a descent in the water table of the liquid-dominated reservoir. For samples collected below the current water level of the well, the minimum values of homogenization temperature (T_h) fit the present thermal profile, whereas minimum T_h values of samples from above the water level are several tens of degrees higher than the present thermal profile and fit a paleo-thermal profile following the boiling point curve for pure water, as adjusted to 92 °C at 20 m below the present land surface. This is attributed to development of an evolving vapor zone that formed subsequent to a sudden drop in the water table of the liquid-dominated reservoir. We suggest that these events were caused by the drainage of an intracaldera lake when the southwestern wall of the caldera was breached about 0.5 Ma. This model indicates that vapor zones above major liquid-dominated geothermal reservoirs can be formed due to dramatic changes in geohydrology and not just from simple boiling.     

Petrographic features of a high-temperature granite just newly solidified magma at the Kakkonda geothermal field, Japan

A 3729-m-deep geothermal research well, WD-1a, provides us with a unique opportunity to study initial petrographic features of a high-temperature granite just after solidification of magma. The well succeeded in collecting three spot-cores of the Kakkonda Granite that is a pluton emplaced at a shallow depth and regarded as a heat source of the active Kakkonda geothermal system. The core samples were collected at the present formation temperatures of 370, 410 and over 500°C. These samples are granodiorite to tonalite consisting mainly of plagioclase, quartz, hornblende, biotite and K-feldspar. A sample collected at a formation temperature of over 500°C possesses the following remarkable petrographic features compared to the other two samples. Interstitial spaces are not completely sealed. K-feldspar exhibits no perthite by the exsolution of albite lamella. Quartz includes glassy melt inclusions without devitrification. Hornblende is less intensively altered to actinolite, and biotite is not altered. This study directly confirmed that perthite in K-feldspar is a recrystallization texture formed at 410–500°C based on a comparison of the in situ temperatures of the samples. Chemical compositions of minerals were analyzed to compare temperatures determined from geothermometers in several publications to the in situ temperatures of the samples.     

Combining ECCI and FIB milling techniques to prepare site-specific TEM samples for crystal defect analysis of deformed minerals at high pressure

Dislocation microstructures in experimentally deformed single-crystal pyrope-rich garnet, (Mg,Fe)₃(Al,Cr)₃Si₃O₁₂, and polycrystalline forsterite, Mg₂SiO₄, were investigated by using electron channeling contrast imaging (ECCI) and transmission electron microscopy (TEM) combined with a focused ion beam (FIB)-microsampling. In the orientation-optimized ECCI method, we successfully observed individual dislocations across subgrain boundaries in a low-atomic-number mineral, pyrope-rich garnet (averaged Z-numbers, AZs ～ 10). Dislocations in a deformed forsterite (iron-free olivine) were also visible in the ECCI. In the ECCI on the single-crystal garnet, deformation bands consisting of dislocations, unusual contrasts in stripes and inhomogeneous distributions of sub-micrometer-sized pores were found. Further site-specific TEM observation on the deformation band revealed a high density of partial dislocations and stacking fault ribbons. The site-specific characterizations from ECCI to TEM, with assistance of FIB, can provide a new approach to investigate dislocation microstructures of deformed materials at high pressure and high temperature.     

Microstructure,composition and P–T conditions of rutile from diamondiferous gneiss of the Saxonian Erzgebirge,Germany

The chemical composition and microstructure of rutile grains in a ultra-high pressure metamorphic gneiss of the Saxonian Erzgebirge, Germany have been studied by Raman spectroscopy, SEM, EMPA and TEM. Rutile inclusions in garnet contain free dislocations, iron-enriched dislocations and exsolved ilmenite lamellae, while subgrain boundaries are observed in rutile grains of the rock matrix. The previously reported α-PbO₂ type TiO₂ phase could not be confirmed by our TEM observations. On the basis of Zr solubility in the rutile and the presence of microdiamonds, minimum metamorphic peak conditions of 3.95 GPa and 915 °C are estimated.